Evidence map›Paper›PMID 20118994›Full record

Trial reportBone marrow transplantation2010

Sequential recovery of NK cell receptor repertoire after allogeneic hematopoietic SCT.

S Giebel, J Dziaczkowska, T Czerw, J Wojnar, M Krawczyk-Kulis, I Nowak, A Holowiecka, A Segatti, S Kyrcz-Krzemien, P Kusnierczyk and 1 more

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Bone marrow transplantation, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.5field-weighted citation impact, top 35% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. NKG2A Expression Is NotFrontiers in immunology · 2018
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

S GiebelDepartment of Clinical and Experimental Oncology, Division of Bone Marrow Transplantation and Lymphoma, Comprehensive Cancer Centre, Maria Sklodowska-Curie Memorial Institute-Gliwice Branch, Gliwice, Poland. sgiebel@io.gliwice.pl
J Dziaczkowska
T Czerw
J Wojnar
M Krawczyk-Kulis
I Nowak
A Holowiecka
A Segatti
S Kyrcz-Krzemien
P Kusnierczyk
J Holowiecki
Medical University of Silesia · PLThe Maria Sklodowska-Curie National Research Institute of Oncology · PLLudwik Hirszfeld Institute of Immunology and Experimental Therapy · PLUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alloreactivity of natural killer (NK) cells contributes to the GVL reaction after allogeneic hematopoietic SCT (allo-HSCT). However, various procedure-related factors may affect NK cell maturation and their ability to recognize and kill leukemic cells. In this study, we prospectively evaluated expression of NK cell inhibitory receptors in 83 adults treated with myeloablative, killer cell Ig-like receptor (KIR)-ligand-matched allo-HSCT. NK cell maturation was evaluated by comparing the phenotypic patterns after allo-HSCT with the donor ones. The frequencies of KIR3DL1 were comparable to the donor ones on day +28, while they decreased significantly starting from day +100. The expression of KIR2DL2/3 was significantly lower in patients compared with donors up to day +100. The expression of KIR2DL1, despite continues growth, remained significantly decreased for 1 year after allo-HSCT. NKG2A was over-expressed up to day +180. Within 1 year after allo-HSCT, the NK cell phenotypic pattern tended to recapitulate the donor type. The process was disturbed by the use of steroids with significant differences observed on days +56 (P=0.01) and +100 (P=0.04). Up to day +100, reconstitution of NK cell receptor repertoire correlated with the absolute numbers of circulating CD3(+), CD3(+)CD4(+) and CD3(+)CD8(+) cells. Our observations should be taken into account when trying to predict potential benefit from NK cell alloreactivity.

Indexed as

RegenerationAdolescentAdultHematologic NeoplasmsHematopoietic Stem Cell TransplantationHumansImmunity, InnateKiller Cells, NaturalMiddle AgedMyeloablative AgonistsProspective StudiesReceptors, KIRReceptors, KIR2DL1Receptors, KIR2DL2Receptors, KIR2DL3Receptors, KIR3DL1KIR2DL1 protein, humanKIR2DL2 protein, humanKIR2DL3 protein, humanKIR3DL1 protein, humanMyeloablative AgonistsReceptors, KIRReceptors, KIR2DL1Receptors, KIR2DL2Receptors, KIR2DL3Receptors, KIR3DL1Receptors, Natural Killer CellSteroids

Identifiers

PMID20118994
OpenAlexW2093070908

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.